Shared genetic architecture and bidirectional clinical risks within the psycho-metabolic nexus.

IF 10.8 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL EBioMedicine Pub Date : 2025-01-01 Epub Date: 2024-12-27 DOI:10.1016/j.ebiom.2024.105530
Xiaonan Guo, Yu Feng, Xiaolong Ji, Ningning Jia, Aierpati Maimaiti, Jianbo Lai, Zheng Wang, Sheng Yang, Shaohua Hu
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Abstract

Background: Increasing evidence suggests a complex interplay between psychiatric disorders and metabolic dysregulations. However, most research has been limited to specific disorder pairs, leaving a significant gap in our understanding of the broader psycho-metabolic nexus.

Methods: This study leveraged large-scale cohort data and genome-wide association study (GWAS) summary statistics, covering 8 common psychiatric disorders and 43 metabolic traits. We introduced a comprehensive analytical strategy to identify shared genetic bases sequentially, from key genetic correlation regions to local pleiotropy and pleiotropic genes. Finally, we developed polygenic risk score (PRS) models to translate these findings into clinical applications.

Findings: We identified significant bidirectional clinical risks between psychiatric disorders and metabolic dysregulations among 310,848 participants from the UK Biobank. Genetic correlation analysis confirmed 104 robust trait pairs, revealing 1088 key genomic regions, including critical hotspots such as chr3: 47588462-50387742. Cross-trait meta-analysis uncovered 388 pleiotropic single nucleotide variants (SNVs) and 126 shared causal variants. Among variants, 45 novel SNVs were associated with psychiatric disorders and 75 novel SNVs were associated with metabolic traits, shedding light on new targets to unravel the mechanism of comorbidity. Notably, RBM6, a gene involved in alternative splicing and cellular stress response regulation, emerged as a key pleiotropic gene. When psychiatric and metabolic genetic information were integrated, PRS models demonstrated enhanced predictive power.

Interpretation: The study highlights the intertwined genetic and clinical relationships between psychiatric disorders and metabolic dysregulations, emphasising the need for integrated approaches in diagnosis and treatment.

Funding: The National Key Research and Development Program of China (2023YFC2506200, SHH). The National Natural Science Foundation of China (82273741, SY).

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共享遗传结构和双向临床风险在心理代谢关系。
背景:越来越多的证据表明精神疾病和代谢失调之间存在复杂的相互作用。然而,大多数研究都局限于特定的疾病对,在我们对更广泛的心理代谢关系的理解上留下了重大的空白。方法:本研究利用大规模队列数据和全基因组关联研究(GWAS)汇总统计,涵盖8种常见精神疾病和43种代谢特征。我们采用综合分析策略,从关键遗传相关区域到局部多效性和多效性基因,依次确定共享遗传基础。最后,我们开发了多基因风险评分(PRS)模型,将这些发现转化为临床应用。研究结果:我们在来自英国生物银行的310,848名参与者中发现了精神疾病和代谢失调之间显著的双向临床风险。遗传相关分析确认了104对稳健性状对,揭示了1088个关键基因组区域,包括chr3: 47588462-50387742等关键热点。跨性状荟萃分析发现388个多效单核苷酸变异(snv)和126个共有的因果变异。在变异中,45种新的snv与精神疾病相关,75种新的snv与代谢特征相关,为揭示共病机制提供了新的靶点。值得注意的是,RBM6是一个参与选择性剪接和细胞应激反应调节的基因,是一个关键的多效基因。当整合精神病学和代谢遗传信息时,PRS模型显示出增强的预测能力。解释:该研究强调了精神疾病和代谢失调之间交织在一起的遗传和临床关系,强调了在诊断和治疗方面需要综合方法。资助项目:国家重点研发计划项目(2023YFC2506200, SHH)。国家自然科学基金(82273741,SY)。
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来源期刊
EBioMedicine
EBioMedicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
17.70
自引率
0.90%
发文量
579
审稿时长
5 weeks
期刊介绍: eBioMedicine is a comprehensive biomedical research journal that covers a wide range of studies that are relevant to human health. Our focus is on original research that explores the fundamental factors influencing human health and disease, including the discovery of new therapeutic targets and treatments, the identification of biomarkers and diagnostic tools, and the investigation and modification of disease pathways and mechanisms. We welcome studies from any biomedical discipline that contribute to our understanding of disease and aim to improve human health.
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